Canonical Allele Identifier: CA12464819
Gene: BLVRA HGNC NCBI

Linked Data

dbSNP Id: rs2877262
gnomAD v2: 7-43841409-G-C
gnomAD v3: 7-43801810-G-C
gnomAD v4: 7-43801810-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.43801810G>C , CM000669.2:g.43801810G>C GRCh38
NC_000007.13:g.43841409G>C , CM000669.1:g.43841409G>C GRCh37
NC_000007.12:g.43807934G>C NCBI36
NG_031876.1:g.48138G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000265523.9:c.460+1238G>C MANE Select ENSP00000265523.4:n.460+1238G>C
ENST00000265523.8:c.460+1238G>C ENSP00000265523.4:n.460+1238G>C
ENST00000402924.5:c.460+1238G>C ENSP00000385757.1:n.460+1238G>C
ENST00000486984.1:n.164+1238G>C
NM_000712.3:c.460+1238G>C NP_000703.2:n.460+1238G>C
NM_001253823.1:c.460+1238G>C NP_001240752.1:n.460+1238G>C
XM_011515474.1:c.460+1238G>C XP_011513776.1:n.460+1238G>C
XR_428136.2:n.265-16052C>G
XR_927212.1:n.265-16052C>G
XR_927213.1:n.265-16052C>G
XM_011515474.3:c.460+1238G>C XP_011513776.1:n.460+1238G>C
XM_017012520.2:c.460+1238G>C XP_016868009.1:n.460+1238G>C
XM_024446867.1:c.460+1238G>C XP_024302635.1:n.460+1238G>C
XR_001745190.1:n.266-16052C>G
NM_000712.4:c.460+1238G>C MANE Select NP_000703.2:n.460+1238G>C
NM_001253823.2:c.460+1238G>C NP_001240752.1:n.460+1238G>C